About: Jamilé Hazan

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About: Jamilé Hazan Goto Sponge NotDistinct Permalink

An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Hazan, Jamilé Hazan, Jamilé
preferred label	Hazan, Jamilé
name	Jamilé Hazan
Language	http://lexvo.org/id/iso639-3/fra
Given name	Jamilé
familyName	Hazan
note	Directeur d'une thèse en Neurosciences à Paris 6 en 2014
gender	female
ORCID iD	0000-0001-8119-0325
Scopus ID	56212990400
is sameAs of	Hazan, Jamilé Hazan, Jamilé
is Thesis advisor of	http://www.sudoc.fr/202452662/id http://www.sudoc.fr/183927028/id http://www.sudoc.fr/250260425/id http://www.sudoc.fr/257167307/id
is Praeses of	http://www.sudoc.fr/275530221/id
is Author of	http://www.sudoc.fr/043914160/id http://www.sudoc.fr/245834893/id Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family BMP- and neuropilin 1-mediated motor axon navigation relies on spastin alternative translation DEVELOPPEMENT D'UNE METHODE D'ANALYSE DES MICROSATELLITES, APPLICATIONS A LA CARTOGRAPHIE DU CHROMOSOME 20 HUMAIN ET A L'ETUDE GENETIQUE DES PARAPLEGIES SPASTIQUES FAMILIALES Microtubule-targeting drugs rescue axonal swellings in cortical neurons from spastin knockout mice Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathy Deleted Chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genes Motor system abnormalities in hereditary spastic paraparesis type 4 (SPG4) depend on the type of mutation in the spastin gene Motor axon navigation relies on Fidgetin-like 1–driven microtubule plus end dynamics Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis FIGNL1 associates with KIF1Bβ and BICD1 to restrict dynein transport velocity during axon navigation Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description.
is primary topic of	http://www.idref.fr/18372142X
is Opponent of	http://www.sudoc.fr/221266674/id
is Thesis referee of	http://www.sudoc.fr/187208638/id http://www.sudoc.fr/226971740/id http://www.sudoc.fr/248967711/id

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